WO2010118367A3 - Pyrimidines antivirales - Google Patents
Pyrimidines antivirales Download PDFInfo
- Publication number
- WO2010118367A3 WO2010118367A3 PCT/US2010/030598 US2010030598W WO2010118367A3 WO 2010118367 A3 WO2010118367 A3 WO 2010118367A3 US 2010030598 W US2010030598 W US 2010030598W WO 2010118367 A3 WO2010118367 A3 WO 2010118367A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compounds
- infection
- pyrimidines
- pyrazolopyrimtdines
- virus
- Prior art date
Links
- 150000003230 pyrimidines Chemical class 0.000 title abstract 3
- 230000000840 anti-viral effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 241000711549 Hepacivirus C Species 0.000 abstract 3
- 208000015181 infectious disease Diseases 0.000 abstract 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical class N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 abstract 1
- 241000710781 Flaviviridae Species 0.000 abstract 1
- 241000700605 Viruses Species 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- -1 pyrazolopyrimtdines Chemical class 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
- 230000009385 viral infection Effects 0.000 abstract 1
- 230000003612 virological effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
- C07D239/545—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/553—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms with halogen atoms or nitro radicals directly attached to ring carbon atoms, e.g. fluorouracil
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La présente invention concerne de nouveaux composés comprenant des pyrimidines, des pyrazolopyrimidines, et des imidazolopyrimidines substituées, leurs synthèses, et des compositions les comprenant, y compris des compositions pharmaceutiques, comprenant les nouvelles pyrimidines, pyrazolopyrimidines, imidazolpyrimidines et des composés analogues. De tels composés fonctionnent en inhibant l'entrée des virus de la famille des Flaviviridae, y compris le virus de l'hépatite C (VHC), à l'intérieur des cellules qui sont susceptibles d'être infectées par les virus. Ces composés sont utiles dans le traitement, la thérapie et/ou la prophylaxie de maladies virales et d'infections, y compris l'infection par le VHC.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16832309P | 2009-04-10 | 2009-04-10 | |
US61/168,323 | 2009-04-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2010118367A2 WO2010118367A2 (fr) | 2010-10-14 |
WO2010118367A3 true WO2010118367A3 (fr) | 2011-03-10 |
Family
ID=42936895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2010/030598 WO2010118367A2 (fr) | 2009-04-10 | 2010-04-09 | Pyrimidines antivirales |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2010118367A2 (fr) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8476282B2 (en) | 2008-11-03 | 2013-07-02 | Intellikine Llc | Benzoxazole kinase inhibitors and methods of use |
US8637542B2 (en) | 2008-03-14 | 2014-01-28 | Intellikine, Inc. | Kinase inhibitors and methods of use |
US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
US9096611B2 (en) | 2008-07-08 | 2015-08-04 | Intellikine Llc | Kinase inhibitors and methods of use |
US9295673B2 (en) | 2011-02-23 | 2016-03-29 | Intellikine Llc | Combination of mTOR inhibitors and P13-kinase inhibitors, and uses thereof |
US9359349B2 (en) | 2007-10-04 | 2016-06-07 | Intellikine Llc | Substituted quinazolines as kinase inhibitors |
US9718825B2 (en) | 2013-03-13 | 2017-08-01 | Sanofi | N-(4-(azaindazol-6-yl)-phenyl)-sulfonamides and their use as pharmaceuticals |
US11730736B2 (en) | 2017-11-06 | 2023-08-22 | Rapt Therapeutics, Inc. | Anticancer agents |
Families Citing this family (83)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG177384A1 (en) | 2009-06-29 | 2012-02-28 | Incyte Corp | Pyrimidinones as pi3k inhibitors |
US8445490B2 (en) | 2009-10-14 | 2013-05-21 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
EP2488526B1 (fr) | 2009-10-14 | 2013-07-24 | Bristol-Myers Squibb Company | Composés utiles pour le traitement de l'hépatite c |
US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
CA2796311A1 (fr) | 2010-04-14 | 2011-10-20 | Incyte Corporation | Derives condenses en tant qu'inhibiteurs de pi3k.sigma. |
EP2566872B1 (fr) | 2010-05-04 | 2014-12-24 | Bristol-Myers Squibb Company | Composés destinés au traitement de l'hépatite c |
US9062055B2 (en) | 2010-06-21 | 2015-06-23 | Incyte Corporation | Fused pyrrole derivatives as PI3K inhibitors |
US8765944B2 (en) | 2010-08-19 | 2014-07-01 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
CA2822070C (fr) | 2010-12-20 | 2019-09-17 | Incyte Corporation | N-(1-(phenyl substitue)ethyl)-9h-purin-6-amines en tant qu'inhibiteurs de pi3k |
WO2012125629A1 (fr) | 2011-03-14 | 2012-09-20 | Incyte Corporation | Dérivés diamino-pyrimidines et diamino-pyridines substituées en tant qu'inhibiteurs de pi3k |
US9126948B2 (en) | 2011-03-25 | 2015-09-08 | Incyte Holdings Corporation | Pyrimidine-4,6-diamine derivatives as PI3K inhibitors |
US8933066B2 (en) | 2011-04-14 | 2015-01-13 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
JP6222776B2 (ja) | 2011-04-21 | 2017-11-01 | オリゲニス ゲーエムベーハーOrigenis Gmbh | キナ−ゼ・インヒビタ−として有用なピラゾロ[4,3−d]ピリミジン |
RS61761B1 (sr) | 2011-09-02 | 2021-05-31 | Incyte Holdings Corp | Heterociklilamini kao inhibitori pi3k |
UA110259C2 (uk) | 2011-09-22 | 2015-12-10 | Пфайзер Інк. | Похідні піролопіримідину і пурину |
US8629150B2 (en) | 2011-09-28 | 2014-01-14 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
US8697706B2 (en) | 2011-10-14 | 2014-04-15 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
US8916702B2 (en) | 2012-02-06 | 2014-12-23 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
WO2013182546A1 (fr) * | 2012-06-07 | 2013-12-12 | F. Hoffmann-La Roche Ag | Inhibiteurs de tankyrase à base de pyrazolopyrimidone et de pyrazolopyridone |
CN102827085A (zh) * | 2012-09-17 | 2012-12-19 | 符爱清 | 2,4,5-三氯嘧啶化合物的制备方法 |
CN102952086B (zh) * | 2012-09-28 | 2013-08-28 | 天津科创医药中间体技术生产力促进有限公司 | 一种2-吗啉基取代嘧啶类化合物的制备方法 |
CN102887860B (zh) * | 2012-09-29 | 2015-07-01 | 上海泰坦科技有限公司 | 4-氯-6-三氟甲基嘧啶类化合物的制备方法 |
EP2917222A1 (fr) | 2012-10-18 | 2015-09-16 | Bristol-Myers Squibb Company | Composés pour le traitement de l'hépatite c |
US9637491B2 (en) * | 2012-10-19 | 2017-05-02 | Origenis Gmbh | Pyrazolo[4,3-D]pyrimidines as kinase inhibitors |
BR112015010412A2 (pt) | 2012-11-08 | 2017-07-11 | Pfizer | compostos heteroaromáticos e seu uso como ligantes de dopamina d1 |
PL2935269T3 (pl) * | 2012-12-20 | 2018-09-28 | Ucb Biopharma Sprl | Terapeutycznie czynne pochodne pirazolo-pirymidyny |
EP2953953B1 (fr) | 2013-02-07 | 2017-11-15 | Bristol-Myers Squibb Company | Molécules macrocycliques utilisées en tant qu'inhibiteurs de la pénétration du vhc |
US9624245B2 (en) | 2013-02-07 | 2017-04-18 | Bristol-Myers Squibb Company | Macrocyclic compounds as HCV entry inhibitors |
JP2016510746A (ja) | 2013-03-07 | 2016-04-11 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎の治療のための化合物 |
WO2014135507A1 (fr) * | 2013-03-07 | 2014-09-12 | F. Hoffmann-La Roche Ag | Nouveaux dérivés de pyrazole |
HUE039589T2 (hu) | 2013-05-02 | 2019-01-28 | Hoffmann La Roche | Purinszármazékok mint CB2 receptor agonisták |
DK2991988T3 (en) | 2013-05-02 | 2017-08-21 | Hoffmann La Roche | Pyrrolo [2,3-d] pyrimidine derivatives as CB2 receptor agonists |
WO2015005491A1 (fr) | 2013-07-12 | 2015-01-15 | 国立大学法人京都大学 | Procédé de criblage d'une substance capable d'inhiber l'épissage anormal provoquant l'apparition ou l'évolution d'une maladie |
EP3057592B1 (fr) * | 2013-10-18 | 2019-05-22 | Indiana University Research and Technology Corporation | Effecteurs d'assemblage de virus de l'hépatite b |
UA115388C2 (uk) | 2013-11-21 | 2017-10-25 | Пфайзер Інк. | 2,6-заміщені пуринові похідні та їх застосування в лікуванні проліферативних захворювань |
CA2939219C (fr) * | 2014-02-11 | 2023-02-28 | Mitokinin Llc | Compositions et procedes les utilisant pour le traitement de maladie neurodegenerative et mitochondriale |
WO2015162518A1 (fr) | 2014-04-25 | 2015-10-29 | Pfizer Inc. | Composes hetero-aromatiques et leur utilisation comme ligands d1 de la dopamine |
CR20160493A (es) | 2014-04-25 | 2016-12-16 | Pfizer | Compuestos heteroaromáticos y su uso como ligandos de dopamina d1 |
US10077277B2 (en) | 2014-06-11 | 2018-09-18 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors |
EP4115882A1 (fr) | 2015-01-16 | 2023-01-11 | The General Hospital Corporation | Composés permettant d'améliorer l'épissage d'arnm |
SMT202100015T1 (it) | 2015-02-27 | 2021-03-15 | Incyte Corp | Sali di nibitore di pi3k e preocessi per la loro preparazione |
EP3283472B1 (fr) | 2015-04-17 | 2021-04-14 | Indiana University Research & Technology Corporation | Effecteurs d'assemblage de virus de l'hépatite b |
US9988401B2 (en) | 2015-05-11 | 2018-06-05 | Incyte Corporation | Crystalline forms of a PI3K inhibitor |
US9732097B2 (en) | 2015-05-11 | 2017-08-15 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
US20180072718A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyridine compounds and uses thereof |
TWI867311B (zh) | 2016-09-09 | 2024-12-21 | 美商英塞特公司 | 吡唑并吡啶化合物及其用途 |
TW201811799A (zh) | 2016-09-09 | 2018-04-01 | 美商英塞特公司 | 吡唑并嘧啶化合物及其用途 |
WO2018049191A1 (fr) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Dérivés de pyrazolopyridone en tant que modulateurs de hpk1 et leurs utilisations pour le traitement du cancer |
KR20190053963A (ko) * | 2016-09-30 | 2019-05-20 | 아사나 바이오사이언시스 엘엘씨 | P2x3 및/또는 p2x2/3 화합물 및 방법 |
US20180228786A1 (en) | 2017-02-15 | 2018-08-16 | Incyte Corporation | Pyrazolopyridine compounds and uses thereof |
CN110312528B (zh) | 2017-02-20 | 2022-02-18 | 国立大学法人京都大学 | 用于起因于剪接异常的遗传性疾病的药物组合物及治疗方法 |
CN107383014B (zh) * | 2017-06-21 | 2019-04-30 | 南方医科大学 | 一种1H-吡唑并[3,4-d]嘧啶类化合物及其制备方法和应用 |
KR20200019228A (ko) | 2017-06-21 | 2020-02-21 | 미토키닌, 인크. | 신경퇴행성 및 미토콘드리아 질환의 치료를 위한 조성물 및 이를 사용하는 방법 |
CN109384782A (zh) | 2017-08-04 | 2019-02-26 | 厦门大学 | 取代五元并六元杂环类化合物、其制备方法、药物组合及其用途 |
WO2019051199A1 (fr) | 2017-09-08 | 2019-03-14 | Incyte Corporation | Composés de 6-cyano-indazole utilisés en tant que modulateurs de kinase 1 progénitrices hématopoïétiques (hpk1) |
CR20200421A (es) | 2018-02-20 | 2021-01-26 | Incyte Corp | Derivados de n-(fenil)-2-(fenil)pirimidina-4-carboxamida y compuestos relacionados como inhibidores hpki para tratar el càncer |
US10745388B2 (en) | 2018-02-20 | 2020-08-18 | Incyte Corporation | Indazole compounds and uses thereof |
US10752635B2 (en) | 2018-02-20 | 2020-08-25 | Incyte Corporation | Indazole compounds and uses thereof |
US11299473B2 (en) | 2018-04-13 | 2022-04-12 | Incyte Corporation | Benzimidazole and indole compounds and uses thereof |
AU2019277560B2 (en) | 2018-06-01 | 2025-04-24 | Incyte Corporation | Dosing regimen for the treatment of PI3K related disorders |
US10899755B2 (en) | 2018-08-08 | 2021-01-26 | Incyte Corporation | Benzothiazole compounds and uses thereof |
MA53726A (fr) | 2018-09-25 | 2022-05-11 | Incyte Corp | Composés pyrazolo[4,3-d]pyrimidine en tant que modulateurs des alk2 et/ou fgfr |
WO2020063636A1 (fr) * | 2018-09-27 | 2020-04-02 | 苏州锐明新药研发有限公司 | Composé de pyrazolopyrimidine et son procédé de préparation et son utilisation dans la préparation d'un médicament anticancéreux |
CN110698432B (zh) * | 2018-11-07 | 2023-02-03 | 中国医学科学院医药生物技术研究所 | 苯甲基哌嗪类化合物及其制备方法和在抗病毒中的应用 |
CN111170992B (zh) * | 2018-11-12 | 2021-05-14 | 新发药业有限公司 | 一种5,6-二氢吡啶-2(1h)-酮衍生物的制备方法 |
US20220024891A1 (en) * | 2018-12-04 | 2022-01-27 | The Board Of Regents Of The University Of Texas System | Therapeutics targeting mutant adenomatous polyposis coli (apc) for the treatment of cancer |
WO2020167628A1 (fr) | 2019-02-13 | 2020-08-20 | Ptc Therapeutics, Inc. | Composés de thioéno[3,2-b]pyridin-7-amine pour le traitement de la dysautonomie familiale |
EP3924050A1 (fr) | 2019-02-13 | 2021-12-22 | PTC Therapeutics, Inc. | Composés de pyrrolo[2,3-d] pyrimidine pour le traitement de la dysautonomie familiale |
AU2020258017B2 (en) * | 2019-04-18 | 2025-05-29 | Université de Liège | New pyrimidine derivatives for prevention and treatment of gram-negative bacterial infection, contamination and fouling |
CN110437253A (zh) * | 2019-08-06 | 2019-11-12 | 复旦大学 | 含联苯结构的二芳基嘧啶并环化合物及其制备方法和用途 |
CN114450276A (zh) | 2019-08-06 | 2022-05-06 | 因赛特公司 | Hpk1抑制剂的固体形式 |
CA3153096A1 (fr) | 2019-09-13 | 2021-03-18 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Inhibiteurs du recepteur de la tyrosine kinase pour le traitement de maladie ou de trouble sensible a la modulation de la proteine kinase |
EP3800188A1 (fr) | 2019-10-02 | 2021-04-07 | Bayer AG | Pyrazolopyrimidines substituées en tant qu'inhibiteurs d'irak4 |
WO2021102600A1 (fr) | 2019-11-29 | 2021-06-03 | 中国医学科学院医药生物技术研究所 | Composé de benzylpipérazine, son procédé de préparation et son application en antivirus |
EP4081528A4 (fr) * | 2019-12-23 | 2024-03-13 | Sanford Burnham Prebys Medical Discovery Institute | Modulateurs d'ectonucléotides pyrophosphatases/phosphodiestérases 1 (enpp1) et leurs utilisations |
CN115989219A (zh) * | 2020-06-29 | 2023-04-18 | 贝凯恩生物医疗技术有限公司 | 用于治疗炎症小体介导的肺部疾病的丙磺舒化合物 |
CN111732575B (zh) * | 2020-08-03 | 2020-12-11 | 北京鑫开元医药科技有限公司 | 一种n-(3-(嘧啶-2-基)苯基)苯磺酰胺类衍生物、药物组合物、制备方法及应用 |
TW202237615A (zh) * | 2020-12-11 | 2022-10-01 | 南韓商日東製藥股份有限公司 | 作為雄激素受體及磷酸二酯酶雙重抑制劑的新穎化合物 |
CN113292452B (zh) * | 2021-06-01 | 2023-03-24 | 山东京博生物科技有限公司 | 一种氰基乙酰胺的合成方法 |
CN113979945A (zh) * | 2021-11-15 | 2022-01-28 | 湖北理工学院 | 一种制备3-氨基吡唑-4-甲酰胺半硫酸盐的新方法 |
WO2024168104A2 (fr) * | 2023-02-09 | 2024-08-15 | Caraway Therapeutics, Inc. | Modulateurs de trpml, leurs compositions et procédés d'utilisation |
WO2024168106A2 (fr) * | 2023-02-09 | 2024-08-15 | Caraway Therapeutics, Inc. | Modulateurs de trpml, leurs compositions et procédés d'utilisation |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5478830A (en) * | 1992-05-29 | 1995-12-26 | The Du Pont Merck Pharmaceutical Company | Fused-ring heterocycles for the treatment of atherosclerosis |
JP2004506737A (ja) * | 2000-08-18 | 2004-03-04 | アグーロン ファーマシューティカルズ,インコーポレイテッド | ピラゾール化合物、薬剤組成物、およびerabまたはhadh2活性の調節または阻害方法 |
WO2005121107A1 (fr) * | 2004-06-09 | 2005-12-22 | F. Hoffmann-La Roche Ag | Pyrazolopyrimidines |
WO2006132460A1 (fr) * | 2005-06-10 | 2006-12-14 | Dong-A Pharmaceutical.Co., Ltd. | Agent pour la prevention et le traitement des maladies du foie contenant un derive de la pyrazolopyrimidine |
-
2010
- 2010-04-09 WO PCT/US2010/030598 patent/WO2010118367A2/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5478830A (en) * | 1992-05-29 | 1995-12-26 | The Du Pont Merck Pharmaceutical Company | Fused-ring heterocycles for the treatment of atherosclerosis |
JP2004506737A (ja) * | 2000-08-18 | 2004-03-04 | アグーロン ファーマシューティカルズ,インコーポレイテッド | ピラゾール化合物、薬剤組成物、およびerabまたはhadh2活性の調節または阻害方法 |
WO2005121107A1 (fr) * | 2004-06-09 | 2005-12-22 | F. Hoffmann-La Roche Ag | Pyrazolopyrimidines |
WO2006132460A1 (fr) * | 2005-06-10 | 2006-12-14 | Dong-A Pharmaceutical.Co., Ltd. | Agent pour la prevention et le traitement des maladies du foie contenant un derive de la pyrazolopyrimidine |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9359349B2 (en) | 2007-10-04 | 2016-06-07 | Intellikine Llc | Substituted quinazolines as kinase inhibitors |
US8637542B2 (en) | 2008-03-14 | 2014-01-28 | Intellikine, Inc. | Kinase inhibitors and methods of use |
US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
US9637492B2 (en) | 2008-03-14 | 2017-05-02 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
US9096611B2 (en) | 2008-07-08 | 2015-08-04 | Intellikine Llc | Kinase inhibitors and methods of use |
US9828378B2 (en) | 2008-07-08 | 2017-11-28 | Intellikine Llc | Kinase inhibitors and methods of use |
US8476282B2 (en) | 2008-11-03 | 2013-07-02 | Intellikine Llc | Benzoxazole kinase inhibitors and methods of use |
US8476431B2 (en) | 2008-11-03 | 2013-07-02 | Itellikine LLC | Benzoxazole kinase inhibitors and methods of use |
US9295673B2 (en) | 2011-02-23 | 2016-03-29 | Intellikine Llc | Combination of mTOR inhibitors and P13-kinase inhibitors, and uses thereof |
US9718825B2 (en) | 2013-03-13 | 2017-08-01 | Sanofi | N-(4-(azaindazol-6-yl)-phenyl)-sulfonamides and their use as pharmaceuticals |
US11730736B2 (en) | 2017-11-06 | 2023-08-22 | Rapt Therapeutics, Inc. | Anticancer agents |
Also Published As
Publication number | Publication date |
---|---|
WO2010118367A2 (fr) | 2010-10-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2010118367A3 (fr) | Pyrimidines antivirales | |
WO2009091388A3 (fr) | Triazines et composés associés présentant une activité antivirale, compositions et procédés associés | |
WO2011041713A3 (fr) | Agents anti-viraux à base de pipérazinyle | |
MX2010009563A (es) | Compuestos quimicos con accion antiviral contra virus de dengue y otros flavivirus. | |
EP2853531A3 (fr) | Composés antiviraux | |
PH12012502343A1 (en) | Antiviral drugs for treatment or prevention of dengue infection | |
WO2008133753A3 (fr) | Composés antiviraux | |
EA201390538A1 (ru) | Противовирусные соединения | |
EA201000556A1 (ru) | Спиропирролидины и их применение для борьбы с инфицированием посредством hcv (вирус гепатита с) и вич (вирус иммунодефицита человека) | |
WO2010081082A3 (fr) | Dérivés de phosphoramidate de composés guanosine nucléoside pour le traitement d'infections virales | |
IL195025A (en) | History of compressed indolubenzazepine with cyclopropyl and pharmaceuticals containing them as an anti-hcv drug | |
TN2012000264A1 (en) | Hepatitis c virus inhibitors | |
TN2012000214A1 (en) | Hepatitis c virus inhibitors | |
MX2011008045A (es) | Inhibidores del virus de la hepatitis c. | |
MY152971A (en) | Hepatitis c virus inhibitors | |
WO2012092484A3 (fr) | Nucléosides puriques substitués, dérivés phosphoramidate et phosphorodiamidate pour le traitement d'infections virales | |
TW200720285A (en) | Nucleoside compounds for treating viral infections | |
ATE475660T1 (de) | Antivirale verbindungen | |
WO2008021936A3 (fr) | Inhibiteurs du virus de l'hépatite c | |
WO2007041487A3 (fr) | Peptides inhibiteurs d'infections virales | |
WO2011106992A8 (fr) | Inhibiteurs de polymérase du virus de l'hépatite c ns5b | |
MX2009009473A (es) | Compuestos para el tratamiento de hepatitis c. | |
WO2010055164A3 (fr) | Nouveaux inhibiteurs de la réplication de flavivirus | |
CA2862755A1 (fr) | Composes antiviraux avec une fraction dibenzooxaheterocycle | |
WO2009094190A3 (fr) | Méthodes de traitement d’infections virales |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10762525 Country of ref document: EP Kind code of ref document: A2 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 10762525 Country of ref document: EP Kind code of ref document: A2 |